Length Polymorphism and Methylation Status of UPS29 Minisatellite of the <i>ACAP3</i> Gene as Molecular Biomarker of Epilepsy. Sex Differences in Seizure Types and Symptoms

• Main Authors: Irina O. Suchkova, Elena V. Borisova, Eugene L. Patkin
• Format: Article
• Language: English
• Published: MDPI AG 2020-12-01
• Series: International Journal of Molecular Sciences
• Subjects: tandem repeats length polymorphism; UPS29; ACAP3; CENTB5; centaurin beta 5; Arf GAPs
• Online Access: https://www.mdpi.com/1422-0067/21/23/9206

Epilepsy<b> </b>is a neurological disease with different clinical forms and inter-individuals heterogeneity, which may be associated with genetic and/or epigenetic polymorphisms of tandem<i>-</i>repeated noncoding DNA. These polymorphisms may serve as predictive biomarkers of various forms of epilepsy. ACAP3 is the protein regulating morphogenesis of neurons and neuronal migration and is an integral component of important signaling pathways. This study aimed to carry out an association analysis of the length polymorphism and DNA methylation of the UPS29 minisatellite of the <i>ACAP3 </i>gene in patients with epilepsy. We revealed an association of short UPS29 alleles with increased risk of development of symptomatic and cryptogenic epilepsy in women, and also with cerebrovascular pathologies, structural changes in the brain, neurological status, and the clinical pattern of seizures in both women and men. The increase of frequency of hypomethylated UPS29 alleles in men with symptomatic epilepsy, and in women with both symptomatic and cryptogenic epilepsy was observed. For patients with hypomethylated UPS29 alleles, we also observed structural changes in the brain, neurological status, and the clinical pattern of seizures. These associations had sex-specific nature similar to a genetic association. In contrast with length polymorphism epigenetic changes affected predominantly the long UPS29 allele. We suppose that genetic and epigenetic alterations UPS29 can modify <i>ACAP3 </i>expression and thereby affect the development and clinical course of epilepsy.